Clinical Genomics Report

Sample: VEP_FILE_APPROACH

VCF Type: vep_annotated

Report Date: 2025-07-06 00:01

Pipeline: Rare Disease Variant Prioritization v2.0

Executive Summary

0

High Priority Variants

0

Medium Priority Variants

3

Low Priority Variants

3

Total Variants

Clinical Interpretation

No high-priority variants identified.
Consider broader analysis or alternative approaches.

Top 20 Prioritized Variants

CHROM POS REF ALT SYMBOL Consequence gnomAD_AF CADD_PHRED REVEL CLIN_SIG pathogenicity_score priority_score
0 1 230710048 A G NaN NaN NaN NaN NaN NaN 0.0 3.0
1 17 43044295 G A NaN NaN NaN NaN NaN NaN 0.0 3.0
2 17 43045677 C T NaN NaN NaN NaN NaN NaN 0.0 3.0

This report is for research purposes. Clinical decisions should involve genetic counseling.